US8551991B2 - 1,2,3,4-tetrahydroquinoxaline derivative having glucocorticoid receptor binding activity - Google Patents

1,2,3,4-tetrahydroquinoxaline derivative having glucocorticoid receptor binding activity Download PDF

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US8551991B2
US8551991B2 US12/225,010 US22501007A US8551991B2 US 8551991 B2 US8551991 B2 US 8551991B2 US 22501007 A US22501007 A US 22501007A US 8551991 B2 US8551991 B2 US 8551991B2
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dihydro
quinoxalin
trimethyl
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US20090111807A1 (en
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Mamoru Matsuda
Toshiyuki Mori
Kenji Kawashima
Minoru Yamamoto
Masatomo Kato
Miwa Takai
Masato Nagatsuka
Sachiko Kobayashi
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Santen Pharmaceutical Co Ltd
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    • C07D241/36—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
    • C07D241/38—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with only hydrogen or carbon atoms directly attached to the ring nitrogen atoms
    • C07D241/46—Phenazines
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    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
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    • A—HUMAN NECESSITIES
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    • C07D241/38—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with only hydrogen or carbon atoms directly attached to the ring nitrogen atoms
    • C07D241/40—Benzopyrazines
    • C07D241/44—Benzopyrazines with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the hetero ring
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    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
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    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07—ORGANIC CHEMISTRY
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    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Definitions

  • the present invention relates to a novel 1,2,3,4-tetrahydroquinoxaline derivative or a salt thereof, which is useful as a pharmaceutical.
  • the derivative has a glucocorticoid receptor binding activity and is useful as a glucocorticoid receptor modulator having a nonsteroidal structure (a glucocorticoid receptor agonist and/or a glucocorticoid receptor antagonist).
  • a glucocorticoid receptor is a 94 kDa ligand-activated intracellular transcriptional factor that is a member of the nuclear receptor superfamily. This receptor is a mediator of glucocorticoid action which effects the metabolism of carbohydrates, proteins, fats and the like, the suppression of the immune or inflammatory responses, the activation of the central nervous system, the regulation of the cardiovascular function and the basal and stress-related homeostasis and the like.
  • glucocorticoid action-related diseases metabolic disorders such as diabetes and obesity, inflammatory diseases such as arthritis, enteritis and chronic obstructive pulmonary diseases, autoimmune diseases such as connective tissue diseases, allergic diseases such as asthma, atopic dermatitis, allergic rhinitis and conjunctivitis, central nervous system diseases such as psychiatric disorders, Alzheimer's disease and drug use disorders, cardiovascular diseases such as hypertension, hypercalcemia, hyperinsulinemia and hyperlipidemia, homeostasis-related diseases causing an abnormality of neuro-immune-endocrine balance, glaucoma and the like are known. (SOUGOU RINSYOU, 54(7), 1951-2076 (2005), JP-A-2002-193955.)
  • a compound having a glucocorticoid receptor binding activity is considered to be useful as a preventive and/or therapeutic agent for these diseases.
  • glucocorticoid receptor agonists synthesized in the living body such as cortisol and corticosterone, synthetic glucocorticoid receptor agonists such as dexamethasone, prednisone and prednisilone, non-selective glucocorticoid receptor antagonists such as RU486 and the like are known. (JP-A-2002-193955)
  • compounds having a 1,2,3,4-tetrahydroquinoxaline structure are disclosed in WO 04/099192 and JP-A-5-148243 and the like.
  • the compounds disclosed in WO 04/099192 are protein thyrosine phosphatase inhibitors essentially having a carboxylic group.
  • a large number of compounds having 1,2,3,4-tetrahydroquinoxaline structure are disclosed as anti-virus agents in JP-A-5-148243.
  • the present compound has not been specifically disclosed in any of patents.
  • the present inventors conducted studies about the synthesis of 1,2,3,4-tetrahydroquinoxaline derivatives having a novel chemical structure, and succeeded in producing a large number of novel compounds. Further, the present inventors studied the pharmacological actions of the derivatives and as a result, they found that the derivatives have a glucocorticoid receptor binding activity and are useful as a pharmaceutical, and thus the present invention has been completed.
  • the present invention relates to a compound represented by the following general formula (1) or a salt thereof (hereinafter referred to as “the present compound”) and a pharmaceutical composition containing the same.
  • a preferred invention in its pharmaceutical use relates to a glucocorticoid receptor modulator, and its target diseases are glucocorticoid receptor-related diseases, that is, metabolic disorders such as diabetes and obesity, inflammatory diseases such as arthritis, enteritis and chronic obstructive pulmonary diseases, autoimmune diseases such as connective tissue diseases, allergic diseases such as asthma, atopic dermatitis, allergic rhinitis and conjunctivitis, central nervous system diseases such as psychiatric disorders, Alzheimer's disease and drug use disorders, cardiovascular diseases such as hypertension, hypercalcemia, hyperinsulinemia and hyperlipidemia, homeostasis-related diseases causing an abnormality of neuro-immune-endocrine balance, glaucoma and the like.
  • a particularly preferred invention is an invention relating to a preventive or a
  • R 1 represents a halogen atom, a lower alkyl group which may have at least a substituent, a lower cycloalkyl group which may have at least a substituent, an aryl group which may have at least a substituent, a heterocyclic group which may have at least a substituent, a hydroxy group, an ester of a hydroxy group, a lower alkoxy group which may have at least a substituent, a lower cycloalkyloxy group which may have at least a substituent, an aryloxy group which may have at least a substituent, a heterocyclic oxy group which may have at least a substituent, a mercapto group, an ester of a mercapto group, a lower alkylthio group which may have at least a substituent, a lower cycloalkylthio group which may have at least a substituent, an arylthio group which may have at least a substituent, a heterocyclic thi
  • p represents an integer of 0 to 5;
  • each R 1 may be the same or different;
  • R 2 represents a halogen atom, a lower alkyl group which may have at least a substituent, a hydroxy group, an ester of a hydroxy group or a lower alkoxy group which may have at least a substituent;
  • q represents an integer of 0 to 2;
  • each R 2 may be the same or different;
  • R 3 represents a hydrogen atom, a lower alkyl group which may have at least a substituent, a lower alkenyl group which may have at least a substituent, a lower alkylcarbonyl group which may have at least a substituent, a lower alkenylcarbonyl group which may have at least a substituent or an arylcarbonyl group which may have at least a substituent;
  • R 4 and R 5 may be the same or different and represent a hydrogen atom, a halogen atom, a lower alkyl group which may have at least a substituent, a lower alkenyl group which may have at least a substituent, a lower alkynyl group which may have at least a substituent, a lower cycloalkyl group which may have at least a substituent, an aryl group which may have at least a substituent or a heterocyclic group which may have at least a substituent;
  • R 4 and R 5 may be combined together to form a 3- to 8-membered lower cycloalkane ring which may have at least a substituent;
  • R 6 represents a hydrogen atom, a lower alkyl group which may have at least a substituent, a lower alkenyl group which may have at least a substituent, a lower alkynyl group which may have at least a substituent, a lower cycloalkyl group which may have at least a substituent, an aryl group which may have at least a substituent or a heterocyclic group which may have at least a substituent;
  • A represents a lower alkylene group which may have at least a substituent
  • R 7 represents OR 8 , NR 8 R 9 , SR 8 , S(O)R 8 or S(O) 2 R 8 ;
  • R 8 and R 9 may be the same or different and represent a hydrogen atom, a lower alkyl group which may have at least a substituent, a lower alkenyl group which may have at least a substituent, a lower alkynyl group which may have at least a substituent, a lower cycloalkyl group which may have at least a substituent, an aryl group which may have at least a substituent, a heterocyclic group which may have at least a substituent, a formyl group, a lower alkylcarbonyl group which may have at least a substituent, a lower alkenylcarbonyl group which may have at least a substituent, a lower alkynylcarbonyl group which may have at least a substituent, a lower cycloalkylcarbonyl group which may have at least a substituent, an arylcarbonyl group which may have at least a substituent, a heterocyclic carbonyl group which may have at least a substituent,
  • R 7 is NR 8 R 9
  • R 8 and R 9 may be combined together to form a 3- to 8-membered nitrogen-containing heterocyclic ring which may have at least a substituent
  • the present invention provides a 1,2,3,4-tetrahydroquinoxaline derivative or a salt thereof, which is useful as a pharmaceutical.
  • the present compound has an excellent glucocorticoid receptor binding activity and is useful as a glucocorticoid receptor modulator.
  • the present compound is useful as a preventive or therapeutic agent for glucocorticoid action related diseases, that is, metabolic disorders such as diabetes and obesity, inflammatory diseases such as arthritis, enteritis and chronic obstructive pulmonary diseases, autoimmune diseases such as connective tissue diseases, allergic diseases such as asthma, atopic dermatitis, allergic rhinitis and conjunctivitis, central nervous system diseases such as psychiatric disorders, Alzheimer's disease and drug use disorders, cardiovascular diseases such as hypertension, hypercalcemia, hyperinsulinemia and hyperlipidemia, homeostasis-related diseases causing an abnormality of neuro-immune-endocrine balance, glaucoma and the like.
  • metabolic disorders such as diabetes and obesity
  • inflammatory diseases such as arthritis, enteritis and chronic obstructive pulmonary diseases
  • autoimmune diseases such as connective tissue diseases
  • allergic diseases such as asthma, atopic dermatitis, allergic rhinitis and conjunctivitis
  • central nervous system diseases such as psychi
  • halogen atom refers to a fluorine, chlorine, bromine or iodine atom.
  • the “lower alkyl group” refers to a straight chain or branched alkyl group having 1 to 8 carbon atoms. Specific examples thereof include methyl, ethyl, n-propyl, n-butyl, n-pentyl, n-hexyl, n-heptyl, n-octyl, isopropyl, isobutyl, sec-butyl, tert-butyl and isopentyl groups and the like.
  • lower alkenyl group refers to a straight chain or branched alkenyl group having 2 to 8 carbon atoms. Specific examples thereof include vinyl, propenyl, butenyl, pentenyl, hexenyl, heptenyl, octenyl, isopropenyl, 2-methyl-1-propenyl and 2-methyl-2-butenyl groups and the like.
  • lower alkynyl group refers to a straight chain or branched alkynyl group having 2 to 8 carbon atoms. Specific examples thereof include ethynyl, propynyl, butynyl, pentynyl, hexynyl, heptynyl, octynyl, isobutynyl and isopentynyl groups and the like.
  • the “lower cycloalkyl group” refers to a cycloalkyl group having 3 to 8 carbon atoms. Specific examples thereof include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl groups.
  • the “lower cycloalkane ring” refers to a cycloalkane ring having 3 to 8 carbon atoms. Specific examples thereof include cyclopropane, cyclobutane, cyclopentane, cyclohexane, cycloheptane and cyclooctane rings.
  • the “aryl group” refers to a residue formed by removing one hydrogen atom from a monocyclic aromatic hydrocarbon group, or bicyclic or tricyclic condensed polycyclic aromatic hydrocarbon having 6 to 14 carbon atoms. Further, A residue formed by removing one hydrogen atom from bicyclic or tricyclic condensed polycyclic hydrocarbon having 6 to 14 carbon atoms is also included in the scope of the “aryl group”. Specific examples thereof include phenyl, naphthyl, anthryl, phenanthryl and fluorenyl groups and the like.
  • heterocyclic group refers to a residue formed by removing one hydrogen atom from a saturated or unsaturated monocyclic heterocyclic ring, or a bicyclic or tricyclic condensed polycyclic heterocyclic ring having one or a plurality of heteroatoms selected from a nitrogen atom, an oxygen atom and a sulfur atom in the ring.
  • saturated monocyclic heterocyclic ring examples include pyrrolidine, pyrazolidine, imidazolidine, triazolidine, piperidine, hexahydropyridazine, hexahydropyrimidine, piperazine, homopiperidine and homopiperazine rings and the like having a nitrogen atom in the ring, tetrahydrofuran and tetrahydropyran rings and the like having an oxygen atom in the ring, tetrahydrothiophene and tetrahydrothiopyran rings and the like having a sulfur atom in the ring, oxazolidine, isoxazolidine and morpholine rings and the like having a nitrogen atom and an oxygen atom in the ring, and thiazolidine, isothiazolidine and thiomorpholine rings and the like having a nitrogen atom and a sulfur atom in the ring.
  • such a saturated monocyclic heterocyclic ring can be condensed with a benzene ring or the like to form a bicyclic or tricyclic condensed polycyclic heterocyclic ring such as a dihydroindole, dihydroindazole, dihydrobenzimidazole, tetrahydroquinoline, tetrahydroisoquinoline, tetrahydrocinnoline, tetrahydrophthalazine, tetrahydroquinazoline, tetrahydroquinoxaline, dihydrobenzofuran, dihydroisobenzofuran, chromane, isochromane, dihydrobenzothiophene, dihydroisobenzothiophene, thiochromane, isothiochromane, dihydrobenzoxazole, dihydrobenzisoxazole, dihydrobenzoxazine, dihydrobenzothiazole, dihydrobenzimi
  • the unsaturated monocyclic heterocyclic ring include dihydropyrrole, pyrrole, dihydropyrazole, pyrazole, dihydroimidazole, imidazole, dihydrotriazole, triazole, tetrahydropyridine, dihydropyridine, pyridine, tetrahydropyridazine, dihydropyridazine, pyridazine, tetrahydropyrimidine, dihydropyrimidine, pyrimidine, tetrahydropyrazine, dihydropyrazine and pyrazine rings and the like having a nitrogen atom in the ring, dihydrofuran, furan, dihydropyran and pyran rings and the like having an oxygen atom in the ring, dihydrothiophene, thiophene, dihydrothiopyran and thiopyran rings and the like having a sulfur atom in the ring, dihydrooxazo
  • an unsaturated monocyclic heterocyclic ring can be condensed with a benzene ring or the like to form a bicyclic or tricyclic condensed polycyclic heterocyclic ring such as an indole, indazole, benzimidazole, benzotriazole, dihydroquinoline, quinoline, dihydroisoquinoline, isoquinoline, phenanthridine, dihydrocinnoline, cinnoline, dihydrophthalazine, phthalazine, dihydroquinazoline, quinazoline, dihydroquinoxaline, quinoxaline, benzofuran, isobenzofuran, chromene, isochromene, benzothiophene, isobenzothiophene, thiochromene, isothiochromene, benzoxazole, benzisoxazole, benzoxazine, benzothiazole, benzisothiazole, be
  • the “lower alkoxy group” refers to a group formed by replacing the hydrogen atom of a hydroxy group with a lower alkyl group. Specific examples thereof include methoxy, ethoxy, n-propoxy, n-butoxy, n-pentoxy, n-hexyloxy, n-heptyloxy, n-octyloxy, isopropoxy, isobutoxy, sec-butoxy, tert-butoxy and isopentoxy groups and the like.
  • lower alkenyloxy group refers to a group formed by replacing the hydrogen atom of a hydroxy group with a lower alkenyl group. Specific examples thereof include vinyloxy, propenyloxy, butenyloxy, pentenyloxy, hexenyloxy, heptenyloxy, octenyloxy, isopropenyloxy, 2-methyl-1-propenyloxy and 2-methyl-2-butenyloxy groups and the like.
  • lower alkynyloxy group refers to a group formed by replacing the hydrogen atom of a hydroxy group with a lower alkynyl group. Specific examples thereof include ethynyloxy, propynyloxy, butynyloxy, pentynyloxy, hexynyloxy, heptynyloxy, octynyloxy, isobutynyloxy and isopentynyloxy groups and the like.
  • lower cycloalkyloxy group refers to a group formed by replacing the hydrogen atom of a hydroxy group with a lower cycloalkyl group. Specific examples thereof include cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, cyclohexyloxy, cycloheptyloxy and cyclooctyloxy groups.
  • aryloxy group refers to a group formed by replacing the hydrogen atom of a hydroxy group with an aryl group. Specific examples thereof include phenoxy, naphthoxy, anthryloxy and phenanthryloxy groups and the like.
  • heterocyclic oxy group refers to a group formed by replacing the hydrogen atom of a hydroxy group with a heterocyclic group.
  • the “lower alkylthio group” refers to a group formed by replacing the hydrogen atom of a mercapto group with a lower alkyl group. Specific examples thereof include methylthio, ethylthio, n-propylthio, n-butylthio, n-pentylthio, n-hexylthio, n-heptylthio, n-octylthio, isopropylthio, isobutylthio, sec-butylthio, tert-butylthio and isopentylthio groups and the like.
  • lower cycloalkylthio group refers to a group formed by replacing the hydrogen atom of a mercapto group with a lower cycloalkyl group. Specific examples thereof include cyclopropylthio, cyclobutylthio, cyclopentylthio, cyclohexylthio, cycloheptylthio and cyclooctylthio groups.
  • arylthio group refers to a group formed by replacing the hydrogen atom of a mercapto group with an aryl group. Specific examples thereof include phenylthio, naphthylthio, anthrylthio and phenanthrylthio groups and the like.
  • heterocyclic thio group refers to a group formed by replacing the hydrogen atom of a mercapto group with a heterocyclic group.
  • lower alkylamino group refers to a group formed by replacing one or both of the hydrogen atoms of an amino group with a lower alkyl group. Specific examples thereof include methylamino, ethylamino, propylamino, dimethylamino, diethylamino and ethyl(methyl)amino groups and the like.
  • lower cycloalkylamino group refers to a group formed by replacing one or both of the hydrogen atoms of an amino group with a lower cycloalkyl group, or a group formed by replacing one of the hydrogen atoms of an amino group with a lower cycloalkyl group and the other hydrogen atom with a lower alkyl group, a lower alkenyl group or a lower alkynyl group.
  • cyclopropylamino cyclobutylamino, cyclopentylamino, cyclohexylamino, cycloheptylamino, cyclooctylamino, dicyclohexylamino, cyclohexyl(methyl)amino, cyclohexyl(vinyl)amino and cyclohexyl(ethynyl)amino groups and the like.
  • arylamino group refers to a group formed by replacing one or both of the hydrogen atoms of an amino group with an aryl group, or a group formed by replacing one of the hydrogen atoms of an amino group with an aryl group and the other hydrogen atom with a lower alkyl group, a lower alkenyl group, a lower alkynyl group or a lower cycloalkyl group.
  • phenylamino examples thereof include phenylamino, naphthylamino, anthrylamino, phenanthrylamino, diphenylamino, methyl(phenyl)amino, ethyl(phenyl)amino, phenyl(vinyl)amino, ethynyl(phenyl)amino and cyclohexyl(phenyl)amino groups and the like.
  • heterocyclic amino group refers to a group formed by replacing one or both of the hydrogen atoms of an amino group with a heterocyclic group, or a group formed by replacing one of the hydrogen atoms of an amino group with a heterocyclic group and the other hydrogen atom with a lower alkyl group, a lower alkenyl group, a lower alkynyl group, a lower cycloalkyl group or an aryl group.
  • the “lower alkylcarbonyl group” refers to a group formed by replacing the hydrogen atom of a formyl group with a lower alkyl group. Specific examples thereof include methylcarbonyl, ethylcarbonyl, n-propylcarbonyl, n-butylcarbonyl, n-pentylcarbonyl, n-hexylcarbonyl, n-heptylcarbonyl, n-octylcarbonyl, isopropylcarbonyl, isobutylcarbonyl, sec-butylcarbonyl, tert-butylcarbonyl and isopentylcarbonyl groups and the like.
  • lower alkenylcarbonyl group refers to a group formed by replacing the hydrogen atom of a formyl group with a lower alkenyl group.
  • Specific examples thereof include vinylcarbonyl, propenylcarbonyl, butenylcarbonyl, pentenylcarbonyl, hexenylcarbonyl, heptenylcarbonyl, octenylcarbonyl, isopropenylcarbonyl, 2-methyl-1-propenylcarbonyl and 2-methyl-2-butenylcarbonyl groups and the like.
  • lower alkynylcarbonyl group refers to a group formed by replacing the hydrogen atom of a formyl group with a lower alkynyl group. Specific examples thereof include ethynylcarbonyl, propynylcarbonyl, butynylcarbonyl, pentynylcarbonyl, hexynylcarbonyl, heptynylcarbonyl, octynylcarbonyl, isobutynylcarbonyl and isopentynylcarbonyl groups and the like.
  • lower cycloalkylcarbonyl group refers to a group formed by replacing the hydrogen atom of a formyl group with a lower cycloalkyl group. Specific examples thereof include cyclopropylcarbonyl, cyclobutylcarbonyl, cyclopentylcarbonyl, cyclohexylcarbonyl, cycloheptylcarbonyl and cyclooctylcarbonyl groups.
  • arylcarbonyl group refers to a group formed by replacing the hydrogen atom of a formyl group with an aryl group. Specific examples thereof include phenylcarbonyl, naphthylcarbonyl, anthrylcarbonyl and phenanthrylcarbonyl groups and the like.
  • heterocyclic carbonyl group refers to a group formed by replacing the hydrogen atom of a formyl group with a heterocyclic group.
  • the “lower alkoxycarbonyl group” refers to a group formed by replacing the hydrogen atom of a formyl group with a lower alkoxy group. Specific examples thereof include methoxycarbonyl, ethoxycarbonyl, n-propoxycarbonyl, n-butoxycarbonyl, n-pentoxycarbonyl, n-hexyloxycarbonyl, n-heptyloxycarbonyl, n-octyloxycarbonyl, isopropoxycarbonyl, isobutoxycarbonyl, sec-butoxycarbonyl, tert-butoxycarbonyl and isopentoxycarbonyl groups and the like.
  • lower alkenyloxycarbonyl group refers to a group formed by replacing the hydrogen atom of a formyl group with a lower alkenyloxy group. Specific examples thereof include vinyloxycarbonyl, propenyloxycarbonyl, butenyloxycarbonyl, pentenyloxycarbonyl, hexenyloxycarbonyl, heptenyloxycarbonyl, octenyloxycarbonyl, isopropenyloxycarbonyl, 2-methyl-1-propenyloxycarbonyl and 2-methyl-2-butenyloxycarbonyl groups and the like.
  • lower alkynyloxycarbonyl group refers to a group formed by replacing the hydrogen atom of a formyl group with a lower alkynyloxy group. Specific examples thereof include ethynyloxycarbonyl, propynyloxycarbonyl, butynyloxycarbonyl, pentynyloxycarbonyl, hexynyloxycarbonyl, heptynyloxycarbonyl, octynyloxycarbonyl, isobutynyloxycarbonyl and isopentynyloxycarbonyl groups and the like.
  • lower cycloalkyloxycarbonyl group refers to a group formed by replacing the hydrogen atom of a formyl group with a lower cycloalkyloxy group. Specific examples thereof include cyclopropyloxycarbonyl, cyclobutyloxycarbonyl, cyclopentyloxycarbonyl, cyclohexyloxycarbonyl, cycloheptyloxycarbonyl and cyclooctyloxycarbonyl groups.
  • aryloxycarbonyl group refers to a group formed by replacing the hydrogen atom of a formyl group with an aryloxy group. Specific examples thereof include phenoxycarbonyl, naphthoxycarbonyl, anthryloxycarbonyl and phenanthryloxycarbonyl groups and the like.
  • heterocyclic oxycarbonyl group refers to a group formed by replacing the hydrogen atom of a formyl group with a heterocyclic oxy group.
  • lower alkylaminocarbonyl group refers to a group formed by replacing the hydrogen atom of a formyl group with a lower alkylamino group. Specific examples thereof include methylaminocarbonyl, ethylaminocarbonyl, propylaminocarbonyl, dimethylaminocarbonyl, diethylaminocarbonyl and ethylmethylaminocarbonyl groups and the like.
  • the “lower alkenylaminocarbonyl group” refers to a group formed by replacing the hydrogen atom of a formyl group with a lower alkenylamino group. Specific examples thereof include vinylaminocarbonyl, propenylaminocarbonyl, butenylaminocarbonyl, pentenylaminocarbonyl, hexenylaminocarbonyl, heptenylaminocarbonyl, octenylaminocarbonyl, isopropenylaminocarbonyl, 2-methyl-1-propenylaminocarbonyl, 2-methyl-2-butenylaminocarbonyl, divinylaminocarbonyl and methyl(vinyl)aminocarbonyl groups and the like.
  • the “lower alkynylaminocarbonyl group” refers to a group formed by replacing the hydrogen atom of a formyl group with a lower alkynylamino group. Specific examples thereof include ethynylaminocarbonyl, propynylaminocarbonyl, butynylaminocarbonyl, pentynylaminocarbonyl, hexynylaminocarbonyl, heptynylaminocarbonyl, octynylaminocarbonyl, isobutynylaminocarbonyl, isopentynylaminocarbonyl, diethynylaminocarbonyl, ethynyl(methyl)aminocarbonyl and ethynyl(vinyl)aminocarbonyl groups and the like.
  • the “lower cycloalkylaminocarbonyl group” refers to a group formed by replacing the hydrogen atom of a formyl group with a lower cycloalkylamino group. Specific examples thereof include cyclopropylaminocarbonyl, cyclobutylaminocarbonyl, cyclopentylaminocarbonyl, cyclohexylaminocarbonyl, cycloheptylaminocarbonyl, cyclooctylaminocarbonyl, dicyclohexylaminocarbonyl, cyclohexyl(methyl)aminocarbonyl, cyclohexyl(vinyl)aminocarbonyl and cyclohexyl(ethynyl)aminocarbonyl groups and the like.
  • arylaminocarbonyl group refers to a group formed by replacing the hydrogen atom of a formyl group with an arylamino group. Specific examples thereof include phenylaminocarbonyl, naphthylaminocarbonyl, anthrylaminocarbonyl, phenanthrylaminocarbonyl, diphenylaminocarbonyl, methylphenylaminocarbonyl ethylphenylaminocarbonyl, phenyl(vinyl)aminocarbonyl, ethynyl(phenyl)aminocarbonyl and cyclohexyl(phenyl)aminocarbonyl groups and the like.
  • heterocyclic aminocarbonyl group refers to a group formed by replacing the hydrogen atom of a formyl group with a heterocyclic amino group.
  • lower alkylsulfonyl group refers to a group formed by replacing the hydroxy group of a sulfonic acid group with a lower alkyl group. Specific examples thereof include methylsulfonyl, ethylsulfonyl, n-propylsulfonyl, n-butylsulfonyl, n-pentylsulfonyl, n-hexylsulfonyl, n-heptylsulfonyl, n-octylsulfonyl, isopropylsulfonyl, isobutylsulfonyl, sec-butylsulfonyl, tert-butylsulfonyl and isopentylsulfonyl groups and the like.
  • lower alkenylsulfonyl group refers to a group formed by replacing the hydroxy group of a sulfonic acid group with a lower alkenyl group.
  • Specific examples thereof include vinylsulfonyl, propenylsulfonyl, butenylsulfonyl, pentenylsulfonyl, hexenylsulfonyl, heptenylsulfonyl, octenylsulfonyl, isopropenylsulfonyl, 2-methyl-1-propenylsulfonyl and 2-methyl-2-butenylsulfonyl groups and the like.
  • lower alkynylsulfonyl group refers to a group formed by replacing the hydroxy group of a sulfonic acid group with a lower alkynyl group. Specific examples thereof include ethynylsulfonyl, propynylsulfonyl, butynylsulfonyl, pentynylsulfonyl, hexynylsulfonyl, heptynylsulfonyl, octynylsulfonyl, isobutynylsulfonyl and isopentynylsulfonyl groups and the like.
  • lower cycloalkylsulfonyl group refers to a group formed by replacing the hydroxy group of a sulfonic acid group with a lower cycloalkyl group. Specific examples thereof include cyclopropylsulfonyl, cyclobutylsulfonyl, cyclopentylsulfonyl, cyclohexylsulfonyl, cycloheptylsulfonyl and cyclooctylsulfonyl groups.
  • arylsulfonyl group refers to a group formed by replacing the hydroxy group of a sulfonic acid group with an aryl group. Specific examples thereof include phenylsulfonyl, naphthylsulfonyl, anthrylsulfonyl and phenanthrylsulfonyl groups and the like.
  • heterocyclic sulfonyl group refers to a group formed by replacing the hydroxy group of a sulfonic acid group with a heterocyclic group.
  • the “3- to 8-membered nitrogen-containing heterocyclic ring” refers to a saturated monocyclic heterocyclic ring containing one or two nitrogen atoms in the ring. Specific examples thereof include aziridine, azetidine, pyrrolidine, piperidine, imidazolidine, pyrazolidine, piperazine and morpholine rings and the like.
  • lower alkylene group refers to a straight chain or branched alkylene group having 1 to 8 carbon atoms. Specific examples thereof include methylene, ethylene, trimethylene, tetramethylene, pentamethylene, hexamethylene, heptamethylene, octamethylene, methylmethylene and ethylmethylene groups and the like.
  • ester of a hydroxy group refers to an ester formed from a hydroxy group and a carboxylic acid and/or a group represented by —OCO—R.
  • R represents a hydrogen atom, a lower alkyl group which may have at least a substituent, a lower alkenyl group which may have at least a substituent, a lower alkynyl group which may have at least a substituent, a lower cycloalkyl group which may have at least a substituent, an aryl group which may have at least a substituent, a heterocyclic group which may have at least a substituent, a lower alkoxy group which may have at least a substituent, a lower alkenyloxy group which may have at least a substituent, a lower alkynyloxy group which may have at least a substituent, a lower cycloalkyloxy group which may have at least a substituent, an aryloxy group which may have at least a substituent, a heterocyclic oxy group which may have at least a substituent, an amino group, a lower alkylamino group which may have at least a substituent, a lower cycloal
  • ester of a mercapto group refers to a thioester formed from a mercapto group and a carboxylic acid and/or a group represented by —SCO—R.
  • R is the same as the above.
  • amide of an amino group refers to an amide formed from an amino group and a carboxylic acid and/or a group represented by —NHCO—R.
  • R is the same as the above.
  • amide of a lower alkylamino group refers to an amide formed from a lower alkylamino group and a carboxylic acid and/or a group represented by —NR′CO—R.
  • R′ represents a lower alkyl group which may have at least a substituent, and R is the same as the above.
  • amide of a lower cycloalkylamino group refers to an amide formed from a lower cycloalkylamino group and a carboxylic acid and/or a group represented by —NR′′CO—R.
  • R′′ represents a lower cycloalkyl group which may have at least a substituent, and R is the same as the above.
  • amide of an arylamino group refers to an amide formed from an arylamino group and a carboxylic acid and/or a group represented by —NR′′′CO—R.
  • R′′′ represents an aryl group which may have at least a substituent, and R is the same as the above.
  • amide of a heterocyclic amino group refers to an amide formed from a heterocyclic amino group and a carboxylic acid and/or a group represented by —NR′′′′CO—R.
  • R′′′′ represents a heterocyclic group which may have at least a substituent, and R is the same for the above.
  • the “carboxylic acid” refers to a saturated aliphatic carboxylic acid, an unsaturated aliphatic carboxylic acid, an aryl carboxylic acid, a heterocyclic carboxylic acid or the like represented by R a COOH (R a represents a hydrogen atom, a lower alkyl group which may have at least a substituent, a lower alkenyl group which may have at least a substituent, a lower alkynyl group which may have at least a substituent, a lower cycloalkyl group which may have at least a substituent, an aryl group which may have at least a substituent, a heterocyclic group which may have at least a substituent and the like).
  • saturated aliphatic carboxylic acids such as formic acid, acetic acid, propionic acid, butyric acid, isobutyric acid, valeric acid, isovaleric acid, pivalic acid, cyclopropanecarboxylic acid, cyclobutanecarboxylic acid, cyclopentanecarboxylic acid and cyclohexanecarboxylic acid; unsaturated aliphatic carboxylic acids such as acrylic acid, propionic acid, crotonic acid, cinnamic acid, cyclopentenecarboxylic acid and cyclohexenecarboxylic acid; aryl carboxylic acids such as benzoic acid, phthalic acid, isophthalic acid, terephthalic acid, naphthoic acid and toluic acid; heterocyclic carboxylic acids such as furancarboxylic acid, thiophenecarboxylic acid, nicotinic acid and isonicotinic acid; and the saturated ali
  • esters of a carboxy group refers to an ester formed from a carboxy group and an alcohol or a phenol.
  • ester of a sulfonic acid group refers to an ester formed from a sulfonic acid group and an alcohol or a phenol.
  • the “alcohol” refers to a saturated aliphatic hydroxy compound, an unsaturated aliphatic hydroxy compound, a heterocyclic hydroxyl compound or the like represented by R b OH (R b represents a lower alkyl group which may have at least a substituent, a lower alkenyl group which may have at least a substituent, a lower alkynyl group which may have at least a substituent, a lower cycloalkyl group which may have at least a substituent, a heterocyclic group which may have at least a substituent or the like).
  • saturated aliphatic hydroxy compounds such as methanol, ethanol, propanol, butanol, isopropanol, cyclopropanol, cyclobutanol, cyclopentanol, cyclohexanol, benzylalcohol and phenethylalcohol
  • unsaturated aliphatic hydroxy compounds such as vinyl alcohol, allylalcohol, propagylalcohol, cyclopentenol and cyclohexenol
  • heterocyclic hydroxy compounds such as hydroxypiperidine and hydroxytetrahydropyran.
  • the “phenol” refers to an aryl hydroxy compound, a heterocyclic hydroxyl compound or the like represented by R c OH (R c represents an aryl group which may have at least a substituent, a heterocyclic group which may have at least a substituent or the like). Specific examples thereof include aryl hydroxyl compounds such as phenol, naphthol, anthrol and phenanthrol; heterocyclic hydroxyl compounds such as hydroxypyridine, hydroxyfuran and hydroxythiophen.
  • amide of a carboxy group refers to an acid amide formed from a carboxy group and an amine.
  • amide of a sulfonic acid group refers to an acid amide formed from a sulfonic acid group and an amine.
  • the “amine” refers to ammonia, a saturated aliphatic amine compound, an unsaturated aliphatic amine compound, an aryl amine compound, a heterocyclic amine compound, a saturated cyclic amine compound or the like represented by HNR d R e (R d and R e may be the same or different and represent a hydrogen atom, a lower alkyl group which may have at least a substituent, a lower alkenyl group which may have at least a substituent, a lower alkynyl group which may have at least a substituent, a lower cycloalkyl group which may have at least a substituent, an aryl group which may have at least a substituent, a heterocyclic group or the like, or R d and R e may be combined together to form a saturated cyclic amine).
  • saturated aliphatic amine compounds such as methylamine, ethylamine, propylamine, pentylamine, dimethylamine, diethylamine, ethylmethylamine, cyclopropylamine, cyclobutylamine, cyclopentylamine, cyclohexylamine, benzylamine and phenetylamine; unsaturated aliphatic amine compounds such as allylamine and propagylamine; aryl amine compounds such as phenylamine, naphthylamine, anthrylamine, phenanthrylamine, diphenylamine, methylphenylamine and ethylphenylamine; heterocyclic amine compounds such as furylamine, thienylamine, pyrrolidylamine, pyridylamine, quinolylamine and methylpyridylamine; saturated cyclic amine compounds such as aziridine, azetidine, pyr
  • lower alkyl group which may have at least a substituent “lower alkenyl group which may have at least a substituent”, “lower alkynyl group which may have at least a substituent”, “lower alkoxy group which may have at least a substituent”, “lower alkylthio group which may have at least a substituent”, “lower alkylamino group which may have at least a substituent”, “lower alkylcarbonyl group which may have at least a substituent”, “lower alkenylcarbonyl group which may have at least a substituent”, “lower alkynylcarbonyl group which may have at least a substituent”, “lower alkoxycarbonyl group which may have at least a substituent”, “lower alkenyloxycarbonyl group which may have at least a substituent”, “lower alkynyloxycarbonyl group which may have at least a substituent”, “lower alkylaminocarbonyl group which may have at least a substitu
  • lower cycloalkyl group which may have at least a substituent “aryl group which may have at least a substituent”, “heterocyclic group which may have at least a substituent”, “lower cycloalkyloxy group which may have at least a substituent”, “aryloxy group which may have at least a substituent”, “heterocyclic oxy group which may have at least a substituent”, “lower cycloalkylthio group which may have at least a substituent”, “arylthio group which may have at least a substituent”, “heterocyclic thio group which may have at least a substituent”, “lower cycloalkylamino group which may have at least a substituent”, “arylamino group which may have at least a substituent”, “heterocyclic amino group which may have at least a substituent”, “lower cycloalkylcarbonyl group which may have at least a substituent”, “arylcarbonyl group which may have at least a
  • a plurality of groups means that each group may be the same or different and the number of groups is preferably 2. Further, a hydrogen atom and a halogen atom are also included in the concept of the “group”.
  • glucocorticoid receptor modulator refers to a modulator that exhibits a pharmaceutical action by binding to glucocorticoid receptor. Examples thereof include glucocorticoid receptor agonists, glucocorticoid receptor antagonists and the like.
  • the “salt” of the present compound is not particularly limited as long as it is a pharmaceutically acceptable salt, and examples thereof include salts with an inorganic acid such as hydrochloric acid, hydrobromic acid, hydroiodic acid, nitric acid, sulfuric acid or phosphoric acid; salts with an organic acid such as acetic acid, fumalic acid, maleic acid, succinic acid, citric acid, tartaric acid, adipic acid, gluconic acid, glucoheptonic acid, glucuronic acid, terephthalic acid, methanesulfonic acid, lactic acid, hippuric acid, 1,2-ethanedisulfonic acid, isethionic acid, lactobionic acid, oleic acid, pamoic acid, polygalacturonic acid, stearic acid, tannic acid, trifluoromethanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic acid, lauryl sul
  • the present compound may be in the form of a hydrate or a solvate.
  • the crystalline polymorphisms thereof are also included in the present invention.
  • Preferred examples of the present compound include compounds in which the respective groups are groups as defined below and salts thereof in the compounds represented by the general formula (1) and salts thereof.
  • R 1 represents a halogen atom, a lower alkyl group, a lower cycloalkyl group, an aryl group, a heterocyclic group, a hydroxy group, an ester of a hydroxy group, a lower alkoxy group, a lower cycloalkyloxy group, an aryloxy group, a heterocyclic oxy group, a mercapto group, an ester of a mercapto group, a lower alkylthio group, a lower cycloalkylthio group, an arylthio group, a heterocyclic thio group, an amino group, a lower alkylamino group, a lower cycloalkylamino group, an arylamino group, a heterocyclic amino group, an amide of an amino group, an amide of a lower alkylamino group, an amide of a lower cycloalkylamino group, an arylamino group, a heterocyclic amino group,
  • R 1 is a lower alkyl group, a lower alkoxy group, a lower alkylthio group, a lower alkylamino group, an amide of a lower alkylamino group, a lower alkylcarbonyl group or a lower alkylsulfonyl group
  • the lower alkyl group, lower alkoxy group, lower alkylthio group, lower alkylamino group, amide of a lower alkylamino group, lower alkylcarbonyl group or lower alkylsulfonyl group may have one or a plurality of groups selected from a halogen atom, a lower cycloalkyl group, an aryl group, a heterocyclic group, a hydroxy group, an ester of a hydroxy group, a lower alkoxy group, a lower alkoxy group substituted with a halogen atom, a lower cycloalkyloxy group, an aryloxy group, a heterocyclic
  • R 1 is a lower cycloalkyl group, an aryl group, a heterocyclic group, a lower cycloalkyloxy group, an aryloxy group, a heterocyclic oxy group, a lower cycloalkylthio group, an arylthio group, a heterocyclic thio group, a lower cycloalkylamino group, an arylamino group, a heterocyclic amino group, an amide of a lower cycloalkylamino group, an amide of an arylamino group, an amide of a heterocyclic amino group, a lower cycloalkylcarbonyl group, an arylcarbonyl group, a heterocyclic carbonyl group, a lower cycloalkylsulfonyl group, an arylsulfonyl group or a heterocyclic sulfonyl group, the lower cycloalkyl group, aryl group, heterocyclic group
  • (a2) p represents an integer of 0 to 3;
  • each R 1 may be the same or different;
  • R 2 represents a halogen atom, a lower alkyl group, a hydroxy group or a lower alkoxy group
  • (a4) q represents an integer of 0 to 2;
  • each R 2 may be the same or different;
  • R 3 represents a hydrogen atom, a lower alkyl group, a lower alkenyl group, a lower alkylcarbonyl group, a lower alkenylcarbonyl group or an arylcarbonyl group;
  • R 3 is a lower alkyl group or a lower alkylcarbonyl group
  • the lower alkyl group or lower alkylcarbonyl group may have one or a plurality of groups selected from a halogen atom and an aryl group as substituents;
  • the arylcarbonyl group may have one or a plurality of groups selected from a halogen atom, a lower alkyl group, a lower alkyl group substituted with a halogen atom, a lower alkoxy group and a lower alkoxy group substituted with a halogen atom as substituents; and/or
  • R 4 and R 5 may be the same or different and represent a hydrogen atom, a halogen atom, a lower alkyl group, a lower cycloalkyl group, aryl or a heterocyclic group;
  • the lower alkyl group may have one or a plurality of groups selected from a halogen atom, a lower cycloalkyl group, an aryl group, a heterocyclic group, a hydroxy group, an ester of a hydroxy group, a lower alkoxy group, a lower alkoxy group substituted with a halogen atom, a lower cycloalkyloxy group, an aryloxy group, a heterocyclic oxy group, a lower alkylthio group, a lower cycloalkylthio group, an arylthio group, a heterocyclic thio group, an amino group, a lower alkylamino group, a lower cycloalkylamino group, an arylamino group, a heterocyclic amino group, an amide of an amino group, an amide of a lower alkylamino group, an amide of a lower cycloalkylamino group, an arylamino group, a hetero
  • R 4 or R 5 is a lower cycloalkyl group, aryl or a heterocyclic group
  • the lower cycloalkyl group, aryl or heterocyclic group may have one or a plurality of groups selected from a halogen atom, a lower alkyl group, a lower alkyl group substituted with a halogen atom, a hydroxy group, an ester of a hydroxy group, a lower alkoxy group, a lower alkoxy group substituted with a halogen atom, a lower alkylthio group, an amino group, a lower alkylamino group, an amide of an amino group, an amide of a lower alkylamino group, a lower alkylcarbonyl group, a carboxy group, an ester of a carboxy group, an amide of a carboxy group, a lower alkylsulfonyl group, a sulfonic acid group, an ester of a sulf
  • R 4 and R 5 may be combined together to form a 3- to 8-membered lower cycloalkane ring;
  • R 6 represents a hydrogen atom, a lower alkyl group, a lower alkenyl group, a lower alkynyl group or a lower cycloalkyl group;
  • R 6 is a lower alkyl group, a lower alkenyl group, a lower alkynyl group or a lower cycloalkyl group
  • the lower alkyl group, lower alkenyl group, lower alkynyl group or lower cycloalkyl group may have one or a plurality of groups selected from a halogen atom and an aryl group as substituents; and/or
  • A represents a lower alkylene group which may be substituted with a hydroxy group or a halogen atom;
  • R 7 represents OR 8 , NR 8 R 9 or SR 8 ;
  • R 8 and R 9 may be the same or different and represent a hydrogen atom, a lower alkyl group, a lower alkenyl group, a lower alkynyl group, a lower cycloalkyl group, an aryl group, a heterocyclic group, a formyl group, a lower alkylcarbonyl group, a lower alkenylcarbonyl group, a lower alkynylcarbonyl group, a lower cycloalkylcarbonyl group, an arylcarbonyl group, a heterocyclic carbonyl group, a carboxy group, a lower alkoxycarbonyl group, a lower alkenyloxycarbonyl group, a lower alkynyloxycarbonyl group, a lower cycloalkyloxycarbonyl group, an aryloxycarbonyl group, a heterocyclic oxycarbonyl group, a lower alkylsulfonyl group, a lower alkenylsulfonyl
  • R 8 or R 9 is a lower alkyl group, a lower alkenyl group, a lower alkynyl group, a lower alkylcarbonyl group, a lower alkenylcarbonyl group, a lower alkynylcarbonyl group, a lower alkoxycarbonyl group, a lower alkenyloxycarbonyl group, a lower alkynyloxycarbonyl group, a lower alkylsulfonyl group, a lower alkenylsulfonyl group, a lower alkynylsulfonyl group, a lower alkylaminocarbonyl group, a lower alkenylaminocarbonyl group or a lower alkynylaminocarbonyl group, the lower alkyl group, lower alkenyl group, lower alkynyl group, lower alkylcarbonyl group, lower alkenylcarbonyl group, lower alkynylcarbonyl group, lower alkoxycarbonyl group
  • R 8 or R 9 is a lower cycloalkyl group, an aryl group, a heterocyclic group, a lower cycloalkylcarbonyl group, an arylcarbonyl group, a heterocyclic carbonyl group, a lower cycloalkyloxycarbonyl group, an aryloxycarbonyl group, a heterocyclic oxycarbonyl group, a lower cycloalkylsulfonyl group, an arylsulfonyl group, a heterocyclic sulfonyl group, a lower cycloalkylaminocarbonyl group, an arylaminocarbonyl group or a heterocyclic aminocarbonyl group, the lower cycloalkyl group, aryl group, heterocyclic group, lower cycloalkylcarbonyl group, arylcarbonyl group, heterocyclic carbonyl group, lower cycloalkyloxycarbonyl group, aryloxycarbonyl group, aryl
  • R 7 is NR 8 R 9
  • R 8 and R 9 may be combined together to form a 5- or 6-membered nitrogen-containing heterocyclic ring;
  • preferred examples include compounds that comprises one or a combination of two or more selected from the above (a1), (a2), (a3), (a4), (a5), (a6), (a7), (a8), (a9) and (a10), and salts thereof.
  • More preferred examples of the present compound include compounds in which the respective groups are groups as defined below and salts thereof in the compounds represented by the general formula (1) and salts thereof.
  • R 1 represents a halogen atom, a lower alkyl group, a hydroxy group, an ester of a hydroxy group, a lower alkoxy group, a lower alkylthio group, an amino group, a lower alkylamino group, an amide of an amino group, an amide of a lower alkylamino group, a lower alkylcarbonyl group, a carboxy group, an ester of a carboxy group, an amide of a carboxy group, a lower alkylsulfonyl group, a nitro group or a cyano group;
  • R 1 is a lower alkyl group, a lower alkoxy group, a lower alkylthio group, a lower alkylamino group, an amide of a lower alkylamino group, a lower alkylcarbonyl group or a lower alkylsulfonyl group
  • the lower alkyl group, lower alkoxy group, lower alkylthio group, lower alkylamino group, amide of a lower alkylamino group, lower alkylcarbonyl group or lower alkylsulfonyl group may have one or a plurality of groups selected from a halogen atom, a lower cycloalkyl group, an aryl group, a heterocyclic group, a hydroxy group, an ester of a hydroxy group, a lower alkoxy group, a lower alkoxy group substituted with a halogen atom, a lower cycloalkyloxy group, an aryloxy group, a heterocyclic
  • (b2) p represents an integer of 0 to 3;
  • each R 1 may be the same or different;
  • R 3 represents a hydrogen atom, a lower alkyl group, a lower alkenyl group, a lower alkylcarbonyl group, a lower alkenylcarbonyl group or an arylcarbonyl group;
  • R 3 is a lower alkyl group
  • the lower alkyl group may have one or a plurality of aryl groups as substituents
  • R 3 is an arylcarbonyl group
  • the arylcarbonyl group may have one or a plurality of groups selected from a halogen atom and a lower alkyl group as substituents; and/or
  • R 4 and R 5 may be the same or different and represent a hydrogen atom, a halogen atom, a lower alkyl group, a lower cycloalkyl group, aryl or a heterocyclic group;
  • the lower alkyl group may have one or a plurality of groups selected from a halogen atom, a hydroxy group, an ester of a hydroxy group, a lower alkoxy group, a lower alkoxy group substituted with a halogen atom, a lower alkylthio group, an amino group, a lower alkylamino group, an amide of an amino group, an amide of a lower alkylamino group, a lower alkylcarbonyl group, a carboxy group, an ester of a carboxy group, an amide of a carboxy group, a nitro group and a cyano group as substituents;
  • R 4 or R 5 is a lower cycloalkyl group, aryl or a heterocyclic group
  • the lower cycloalkyl group, aryl or heterocyclic group may have one or a plurality of groups selected from a halogen atom, a lower alkyl group, a lower alkyl group substituted with a halogen atom, a hydroxy group, an ester of a hydroxy group, a lower alkoxy group, a lower alkoxy group substituted with a halogen atom, a lower alkylthio group, an amino group, a lower alkylamino group, an amide of an amino group, an amide of a lower alkylamino group, a lower alkylcarbonyl group, a carboxy group, an ester of a carboxy group, an amide of a carboxy group, a lower alkylsulfonyl group, a nitro group and a cyano group as substituents;
  • R 4 and R 5 may be combined together to form a 3- to 8-membered lower cycloalkane ring;
  • R 6 represents a hydrogen atom, a lower alkyl group, a lower alkenyl group, a lower alkynyl group or a lower cycloalkyl group;
  • R 6 is a lower alkyl group, a lower alkenyl group, a lower alkynyl group or a lower cycloalkyl group
  • the lower alkyl group, lower alkenyl group, lower alkynyl group or lower cycloalkyl group may have one or a plurality of groups selected from a halogen atom and an aryl group as substituents; and/or
  • (b7) A represents a lower alkylene group
  • R 7 represents OR 8 , NR 8 R 9 or SR 8 ;
  • R 8 and R 9 may be the same or different and represent a hydrogen atom, a lower alkyl group, a lower alkenyl group, a lower alkynyl group, a lower cycloalkyl group, an aryl group, a heterocyclic group, a formyl group, a lower alkylcarbonyl group, a lower alkenylcarbonyl group, a lower alkynylcarbonyl group, a lower cycloalkylcarbonyl group, an arylcarbonyl group, a heterocyclic carbonyl group, a carboxy group, a lower alkoxycarbonyl group, a lower alkenyloxycarbonyl group, a lower alkynyloxycarbonyl group, a lower cycloalkyloxycarbonyl group, an aryloxycarbonyl group, a heterocyclic oxycarbonyl group, a lower alkylsulfonyl group, a lower alkenylsulfonyl
  • R 8 or R 9 is a lower alkyl group, a lower alkenyl group, a lower alkynyl group, a lower alkylcarbonyl group, a lower alkenylcarbonyl group, a lower alkynylcarbonyl group, a lower alkoxycarbonyl group, a lower alkenyloxycarbonyl group, a lower alkynyloxycarbonyl group, a lower alkylsulfonyl group, a lower alkenylsulfonyl group, a lower alkynylsulfonyl group, a lower alkylaminocarbonyl group, a lower alkenylaminocarbonyl group or a lower alkynylaminocarbonyl group, the lower alkyl group, lower alkenyl group, lower alkynyl group, lower alkylcarbonyl group, lower alkenylcarbonyl group, lower alkynylcarbonyl group, lower alkoxycarbonyl group
  • R 8 or R 9 is a lower cycloalkyl group, an aryl group, a heterocyclic group, a lower cycloalkylcarbonyl group, an arylcarbonyl group, a heterocyclic carbonyl group, a lower cycloalkyloxycarbonyl group, an aryloxycarbonyl group, a heterocyclic oxycarbonyl group, a lower cycloalkylsulfonyl group, an arylsulfonyl group, a heterocyclic sulfonyl group, a lower cycloalkylaminocarbonyl group, an arylaminocarbonyl group or a heterocyclic aminocarbonyl group, the lower cycloalkyl group, aryl group, heterocyclic group, lower cycloalkylcarbonyl group, arylcarbonyl group, heterocyclic carbonyl group, lower cycloalkyloxycarbonyl group, aryloxycarbonyl group, aryl
  • R 7 is NR 8 R 9
  • R 8 and R 9 may be combined together to form a 5- or 6-membered nitrogen-containing heterocyclic ring;
  • more preferred examples include compounds that comprises one or a combination of two or more selected from the above (b1), (b2), (b3), (b4), (b5), (b6), (b7), (b8) and (b9), and salts thereof.
  • R 1 represents a halogen atom, a lower alkyl group, a hydroxy group, an ester of a hydroxy group, a lower alkoxy group, a lower alkylthio group, an amino group, an amide of an amino group, an amide of a lower alkylamino group, a lower alkylcarbonyl group, a carboxy group, an ester of a carboxy group, a nitro group or a cyano group;
  • R 1 is a lower alkyl group or a lower alkoxy group
  • the lower alkyl group or lower alkoxy group may have one or a plurality of groups selected from a halogen atom, a hydroxy group and a lower alkoxy group as substituents; and/or
  • (c2) p represents 1, 2 or 3;
  • each R 1 may be the same or different;
  • R 3 represents a hydrogen atom
  • R 4 and R 5 may be the same or different and represent a lower alkyl group
  • R 6 represents a hydrogen atom, a lower alkyl group or a lower alkenyl group
  • (c7) A represents a lower alkylene group
  • R 7 represents OR 8 or NR 8 R 9 ;
  • R 8 and R 9 may be the same or different and represent a hydrogen atom, an aryl group, an arylcarbonyl group or a heterocyclic carbonyl group;
  • R 8 or R 9 is an aryl group, an arylcarbonyl group or a heterocyclic carbonyl group
  • the aryl group, arylcarbonyl group or heterocyclic carbonyl group may have one or a plurality of groups selected from a halogen atom, a lower alkyl group, a lower alkyl group substituted with at least a halogen atom, a lower alkyl group substituted with at least a hydroxy group, a lower alkenyl group, an aryl group, a lower alkoxy group, a lower alkylcarbonyl group, an ester of a carboxy group, a nitro group and a cyano group as substituents; and/or
  • further more preferred examples include compounds that comprises one or a combination of two or more selected from the above (c1), (c2), (c3), (c4), (c5), (c6), (c7), (c8) and (c9), and salts thereof.
  • R 1 represents a halogen atom, a hydroxy group, an ester of a hydroxy group, a lower alkoxy group, an amide of an amino group or an amide of a lower alkylamino group;
  • each R 1 may be the same or different;
  • R 3 represents a hydrogen atom
  • R 4 and R 5 may be the same or different and represent a lower alkyl group
  • R 6 represents a lower alkyl group
  • (d7) A represents a lower alkylene group
  • R 7 represents OR 8 or NR 8 R 9 ;
  • R 8 represents an aryl group, an arylcarbonyl group or a heterocyclic carbonyl group, in this case, the aryl group, arylcarbonyl group or heterocyclic carbonyl group may have one or a plurality of groups selected from a halogen atom, a lower alkyl group, a lower alkyl group substituted with at least a halogen atom, a lower alkyl group substituted with at least a hydroxy group, a lower alkenyl group, an aryl group, a lower alkoxy group, a lower alkylcarbonyl group, an ester of a carboxy group, a nitro group and a cyano group as substituents;
  • R 9 represents a hydrogen atom
  • further more preferred examples include compounds that comprises one or a combination of two or more selected from the above (d1), (d2), (d3), (d4), (d5), (d6), (d7), (d8) and (d9), and salts thereof.
  • R 1 in the present compound include compounds that satisfy the following requirement and salts thereof.
  • R 1 represents a halogen atom, a hydroxy group, an ester of a hydroxy group, a lower alkoxy group, an amide of an amino group or an amide of a lower alkylamino group, and satisfies the requirement of the above (a), (b) and/or (c).
  • R 4 , R 5 and R 6 in the present compound include compounds that satisfy the following requirement and salts thereof.
  • R 4 , R 5 and R 6 each represent a methyl group, and satisfies the requirement of the above (a), (b), (c) and/or (d).
  • R 8 in the present compound include compounds that satisfy the following requirement and salts thereof.
  • R 8 represents an aryl group, an arylcarbonyl group or a heterocyclic carbonyl group, and the aryl group represents a phenyl group, the arylcarbonyl group represents a phenylcarbonyl group, and/or the heterocyclic carbonyl group represents a thiophenecarbonyl group, and satisfies the requirement of the above (a), (b), (c) and/or (d).
  • Preferred examples of A in the present compound include compounds that satisfy the following requirement and salts thereof.
  • a compound or a salt thereof wherein in the general formula (1), A represent a methylene group, and satisfies the requirement of the above (a), (b), (c) and/or (d).
  • R 1 is an ester of a hydroxyl group in the present compound
  • R 1 is an ester of a hydroxyl group in the present compound
  • the ester of a hydroxy group represents —OCO—R a1 , in which the R a1 represents a hydrogen atom, a lower alkyl group which may have at least a substituent, a lower alkenyl group which may have at least a substituent, a lower alkynyl group which may have at least a substituent, a lower cycloalkyl group which may have at least a substituent, an aryl group which may have at least a substituent, a heterocyclic group which may have at least a substituent, a lower alkoxy group which may have at least a substituent, a lower alkenyloxy group which may have at least a substituent, a lower alkynyloxy group which may have at least a substituent, a lower cycloalkyloxy group which may have at least a substituent, an aryloxy group which may have at least a substituent, a heterocyclic oxy group which may have at at least a substituent, a
  • the R a1 represents a hydrogen atom, a lower alkyl group, a lower alkenyl group, a lower cycloalkyl group, an aryl group, a heterocyclic group, a lower alkoxy group, a lower alkenyloxy group, a lower cycloalkyloxy group, an aryloxy group, a heterocyclic oxy group, an amino group, a lower alkylamino group, a lower cycloalkylamino group, an arylamino group or a heterocyclic amino group;
  • R a1 is a lower alkyl group, a lower alkenyl group, a lower alkoxy group, a lower alkenyloxy group or a lower alkylamino group
  • the lower alkyl group, lower alkenyl group, lower alkoxy group, lower alkenyloxy group or lower alkylamino group may have one or a plurality of groups selected from a halogen atom, an aryl group, a heterocyclic group, a hydroxy group, an ester of a hydroxy group, an amino group, a lower alkylamino group, a carboxy group and an ester of a carboxy group as substituents; and
  • R a1 is a lower cycloalkyl group, an aryl group, a heterocyclic group, a lower cycloalkyloxy group, an aryloxy group, a heterocyclic oxy group, a lower cycloalkylamino group, an arylamino group or a heterocyclic amino group
  • the lower cycloalkyl group, aryl group, heterocyclic group, lower cycloalkyloxy group, aryloxy group, heterocyclic oxy group, lower cycloalkylamino group, arylamino group or heterocyclic amino group may have one or a plurality of groups selected from a halogen atom, a lower alkyl group, a lower alkyl group substituted with at least a halogen atom, a hydroxy group, an ester of a hydroxy group, a lower alkoxy group, a mercapto group, a lower alkylthio group, a formyl group, a
  • the R a1 represents a lower alkyl group, a lower alkenyl group, a lower cycloalkyl group, an aryl group, a heterocyclic group, a lower alkoxy group, an aryloxy group, a lower alkylamino group, a lower cycloalkylamino group, an arylamino group or a heterocyclic amino group;
  • R a1 is a lower alkyl group
  • the lower alkyl group may have one or a plurality of groups selected from an aryl group and a lower alkylamino group as substituents;
  • the aryl group may have one or a plurality of groups selected from a halogen atom, a lower alkyl group, a lower alkyl group substituted with at least a halogen atom, an ester of a hydroxy group, a lower alkoxy group, a lower alkylthio group, a lower alkylcarbonyl group, an ester of a carboxy group and a nitro group as substituents;
  • the heterocyclic group may have one or a plurality of groups selected from a halogen atom, a lower alkyl group, a hydroxy group and a lower alkoxy group as substituents;
  • R a1 is a lower alkylamino group
  • the lower alkylamino group may have one or a plurality of groups selected from an aryl group, a heterocyclic group and an ester of a carboxy group as substituents;
  • the arylamino group may have one or a plurality of groups selected from a halogen atom, a lower alkyl group and a lower alkoxy group as substituents, and satisfies the requirement of the above (a), (b), (c) (d) and/or (e).
  • R 1 is an amide of an amino group in the present compound
  • R 1 is an amide of an amino group in the present compound
  • the amide of an amino group represents —NHCO—R b , in which the R b1 represents a hydrogen atom, a lower alkyl group which may have at least a substituent, a lower alkenyl group which may have at least a substituent, a lower alkynyl group which may have at least a substituent, a lower cycloalkyl group which may have at least a substituent, an aryl group which may have at least a substituent, a heterocyclic group which may have at least a substituent, a lower alkoxy group which may have at least a substituent, a lower alkenyloxy group which may have at least a substituent, a lower alkynyloxy group which may have at least a substituent, a lower cycloalkyloxy group which may have at least a substituent, an aryloxy group which may have at least a substituent, a heterocyclic oxy group which may have at least a a
  • R b1 is a lower alkyl group, a lower alkenyl group, a lower alkoxy group, a lower alkenyloxy group or a lower alkylamino group
  • the lower alkyl group, lower alkenyl group, lower alkoxy group, lower alkenyloxy group or lower alkylamino group may have one or a plurality of groups selected from a halogen atom, an aryl group, a heterocyclic group, a hydroxy group, an ester of a hydroxy group, an amino group, a lower alkylamino group, a carboxy group and an ester of a carboxy group as substituents; and
  • R b1 is a lower cycloalkyl group, an aryl group, a heterocyclic group, a lower cycloalkyloxy group, an aryloxy group, a heterocyclic oxy group, a lower cycloalkylamino group, an arylamino group or a heterocyclic amino group
  • the lower cycloalkyl group, aryl group, heterocyclic group, lower cycloalkyloxy group, aryloxy group, heterocyclic oxy group, lower cycloalkylamino group, arylamino group or heterocyclic amino group may have one or a plurality of groups selected from a halogen atom, a lower alkyl group, a lower alkyl group substituted with at least a halogen atom, a hydroxy group, an ester of a hydroxy group, a lower alkoxy group, a mercapto group, a lower alkylthio group, a formyl group, a
  • the R b1 represents a lower alkyl group, an aryl group, a heterocyclic group, an aryloxy group, a lower alkylamino group or an arylamino group;
  • R b1 is a lower alkyl group
  • the lower alkyl group may have one or a plurality of amino groups as substituents
  • the aryl group may have one or a plurality of groups selected from a halogen atom, a lower alkyl group, a lower alkyl group substituted with at least a halogen atom, an ester of a hydroxy group, a lower alkoxy group, a lower alkylthio group, a lower alkylcarbonyl group, an ester of a carboxy group and a nitro group as substituents;
  • the heterocyclic group may have one or a plurality of groups selected from a halogen atom, a lower alkyl group, a hydroxy group and a lower alkoxy group as substituents;
  • the lower alkylamino group may have one or a plurality of aryl groups as substituents, and satisfies the requirement of the above (a), (b), (c) (d) and/or (e).
  • R 1 is an amide of a lower alkylamino group in the present compound
  • R 1 is an amide of a lower alkylamino group in the present compound
  • the amide of a lower alkylamino group represents —NR c1 CO—R c2 , in which the R c1 represents a lower alkyl group which may have at least a substituent, and the R c2 represents a hydrogen atom, a lower alkyl group which may have at least a substituent, a lower alkenyl group which may have at least a substituent, a lower alkynyl group which may have at least a substituent, a lower cycloalkyl group which may have at least a substituent, an aryl group which may have at least a substituent, a heterocyclic group which may have at least a substituent, a lower alkoxy group which may have at least a substituent, a lower alkenyloxy group which may have at least a substituent, a lower alkynyloxy group which may have at least a substituent, a lower cycloalkyloxy group which may have at least a
  • the R c1 represents a lower alkyl group
  • the R c2 represents a hydrogen atom, a lower alkyl group, a lower alkenyl group, a lower cycloalkyl group, an aryl group, a heterocyclic group, a lower alkoxy group, a lower alkenyloxy group, a lower cycloalkyloxy group, an aryloxy group, a heterocyclic oxy group, an amino group, a lower alkylamino group, a lower cycloalkylamino group, an arylamino group or a heterocyclic amino group;
  • R c2 is a lower alkyl group, a lower alkenyl group, a lower alkoxy group, a lower alkenyloxy group or a lower alkylamino group
  • the lower alkyl group, lower alkenyl group, lower alkoxy group, lower alkenyloxy group or lower alkylamino group may have one or a plurality of groups selected from a halogen atom, an aryl group, a heterocyclic group, a hydroxy group, an ester of a hydroxy group, an amino group, a lower alkylamino group, a carboxy group and an ester of a carboxy group as substituents; and
  • R c2 is a lower cycloalkyl group, an aryl group, a heterocyclic group, a lower cycloalkyloxy group, an aryloxy group, a heterocyclic oxy group, a lower cycloalkylamino group, an arylamino group or a heterocyclic amino group
  • the lower cycloalkyl group, aryl group, heterocyclic group, lower cycloalkyloxy group, aryloxy group, heterocyclic oxy group, lower cycloalkylamino group, arylamino group or heterocyclic amino group may have one or a plurality of groups selected from a halogen atom, a lower alkyl group, a lower alkyl group substituted with at least a halogen atom, a hydroxy group, an ester of a hydroxy group, a lower alkoxy group, a mercapto group, a lower alkylthio group, a formyl group, a
  • the R c represents a lower alkyl group
  • the R c2 represents, a lower alkyl group, an aryl group or a heterocyclic group
  • R c2 is a lower alkyl group
  • the lower alkyl group may have one or a plurality of amino groups as substituents
  • the aryl group may have one or a plurality of groups selected from a halogen atom, a lower alkyl group, a lower alkyl group substituted with at least a halogen atom, an ester of a hydroxy group, a lower alkoxy group, a lower alkylthio group, a lower alkylcarbonyl group, an ester of a carboxy group and a nitro group as substituents;
  • the heterocyclic group may have one or a plurality of groups selected from a halogen atom, a lower alkyl group, a hydroxy group and a lower alkoxy group as substituents;
  • the lower alkylamino group may have one or a plurality of aryl groups as substituents, and satisfies the requirement of the above (a), (b), (c) (d) and/or (e).
  • Particularly preferred specific examples of the present compound include the following compounds and salts thereof.
  • the present compound can be synthesized according to the following procedures.
  • the individual concrete preparation procedures are explained in details in the following examples, [preparation examples]. These examples are intended to make the present invention more clearly understandable, and do not limit the scope of the present invention.
  • the Hal shown in the following synthetic routes represents a halogen atom
  • MOM represents methoxymethyl group
  • Fmoc represents 9-fluorenylmethoxycarbonyl group.
  • the present compound (I)-(a) (the compound that A is methylene group, X is O in the general formula (1)) can be synthesized according to the synthetic route 1. Namely, the compound (I)-(a) can be given by the reaction of the present compound (I)-(b) (the compound that A is methylene group, X is O, R 6 is H in the general formula (1)) with a corresponding halide (II) in an organic solvent such as N,N-dimethylformamide (hereinafter referred to as DMF), tetrahydrofuran (hereinafter referred to as THF), 1,4-dioxane, methylene dichloride in the presence of a base such as cesium carbonate, potassium carbonate at 0° C. to 50° C. for 1 hour to 24 hours.
  • a base such as cesium carbonate, potassium carbonate at 0° C. to 50° C. for 1 hour to 24 hours.
  • the present compound (I)-(b) (the compound that A is methylene group, X is O, R 6 is H, R 7 is OR 8 , NR 8 R 9 or SR 8 in the general formula (1)) can be synthesized according to the synthetic route 2.
  • the compound (I)-(b) can be given by the reaction of the compound (III) with a corresponding alcohol, carboxylic acid, phenol, amine, thiol, thiophenol and the like (IV) in an organic solvent such as DMF, THF, ethanol in the presence of a base such as potassium carbonate, sodium hydride at 0° C. to 100° C. for 1 hour to 48 hours.
  • the present compound (I)-(c) (the compound that A is methylene group, X is O, R 7 is OR 8 in the general formula (1)) can be synthesized according to the synthetic route 3. Namely, the compound (I)-(c) can be given by the reaction of the compound (V) with a corresponding halide (VI) in an organic solvent such as DMF, THF, methylene dichloride in the presence of a base such as triethylamine, potassium carbonate at 0° C. to 50° C. for 1 hour to 48 hours.
  • an organic solvent such as DMF, THF, methylene dichloride
  • a base such as triethylamine
  • the compound (III) and (V) can be synthesized according to the synthetic route 4.
  • the compound (IX) can be given by the reaction of the compound (VII) with a corresponding boronic acid or its ester (VIII) in a solvent such as DMF, 1,4-dioxane, ethanol, toluene, water and in the presence of a base such as cesium carbonate, sodium carbonate, sodium hydrogen carbonate, tripotassium phosphate and a catalyst such as bis(triphenylphosphine)palladium (II) dichloride, tetrakis(triphenylphosphine)palladium (0) at 50° C. to 120° C. for 1 hour to 48 hours.
  • the compound (V) can be given by the treatment of the compound (IX) in an organic solvent such as diethylether, THF in the presence of a reductive agent such as lithium aluminium hydride at ⁇ 30° C. to room temperature for 1 hour to 24 hours.
  • the compound (III) can be given by the treatment of the compound (V) with methanesulfonyl chloride in an organic solvent such as methylene dichloride, THF in the presence of a base such as triethylamine, diisopropylethylamine (hereinafter referred to as DIEA) at 0° C. to room temperature for 30 minutes to 12 hours.
  • DIEA diisopropylethylamine
  • the compound (VII) can be synthesized according to the synthetic route 5.
  • the compound (XI) can be given by the treatment of the compound (X) in an organic solvent such as methanol, ethanol, DMF in the presence of a reductive agent such as tin(II) chloride, ferric(II) chloride at 50° C. to 120° C. for 1 hour to 12 hours.
  • the compound (XII) can be given by the treatment of the compound (XI) with an acetylation agent such as acetyl chloride, acetic anhydride in an organic solvent such as methylene dichloride, THF in the presence of a base such as triethylamine, DIEA at 0° C. to 50° C.
  • the compound (XIII) can be given by the treatment of the compound (XII) with nitric acid in a solvent such as water in the presence of an acid such as sulfuric acid at ⁇ 20° C. to room temperature for 30 minutes to 12 hours.
  • the compound (XIV) can be given by the treatment of the compound (XIII) in an organic solvent such as methanol in the presence of an acid such as boron trifluoride ether complex at 50° C. to the temperature under reflux for 1 hour to 12 hours.
  • the compound (XVI) can be given by the reaction of the compound (XIV) with a corresponding halide (XV) in the presence of a base such as cesium carbonate, potassium carbonate at 50° C. to 120° C. for 1 hour to 120 hours.
  • a base such as cesium carbonate, potassium carbonate
  • the compound (VII) can be given by the treatment of the compound (XVI) in an organic solvent such as methanol, ethanol, DMF in the presence of a reductive agent such as tin(II) chloride, ferric(II) chloride at 50° C. to 120° C. for 1 hour to 12 hours.
  • the present compound (I)-(a) (the compound that A is methylene group, X is O in the general formula (1)) can be also synthesized according to the synthetic route 6. Namely, the compound (I)-(a) can be given by the reaction of the compound (XVII) with a corresponding boronic acid or its ester (VIII) in a solvent such as DMF, 1,4-dioxane, ethanol, toluene, water and in the presence of a base such as cesium carbonate, sodium carbonate, sodium hydrogen carbonate, tripotassium phosphate and a catalyst such as bis(triphenylphosphine)palladium (II) dichloride, tetrakis(triphenylphosphine)palladium (0) at 50° C. to 120° C. for 1 hour to 48 hours.
  • a solvent such as DMF, 1,4-dioxane, ethanol, toluene
  • a base such as cesium carbonate, sodium
  • the present compound (I)-(a) (the compound that A is methylene group, X is O in the general formula (1)) can be also synthesized according to the synthetic route 7.
  • the compound (I)-(a) can be given by the reaction of the compound (XVIII) with a corresponding halide (XIX) in a solvent such as DMF, 1,4-dioxane, ethanol, toluene, water and in the presence of a base such as cesium carbonate, sodium carbonate, sodium hydrogen carbonate, tripotassium phosphate and a catalyst such as bis(triphenylphosphine)palladium (II) dichloride, tetrakis(triphenylphosphine)palladium (0) at 50° C. to 120° C. for 1 hour to 48 hours.
  • a solvent such as DMF, 1,4-dioxane, ethanol, toluene
  • a base such as cesium carbonate, sodium carbonate, sodium hydrogen
  • the compound (XVII) and (XVIII) can be synthesized according to the synthetic route 8. Namely, the compound (XX) can be given by the treatment of the compound (VII) in an organic solvent such as diethylether, THF in the presence of a reductive agent such as lithium aluminium hydride at 0° C. to 50° C. for 1 hour to 24 hours.
  • the compound (XXI) can be given by the reaction of the compound (XX) with a corresponding halide (II) in an organic solvent such as DMF, THF, 1,4-dioxane, methylene dichloride in the presence of a base such as cesium carbonate, potassium carbonate at 0° C. to 50° C. for 1 hour to 24 hours.
  • the compound (XXII) can be given by the treatment of the compound (XXI) with methanesulfonyl chloride in an organic solvent such as methylene dichloride, THF in the presence of a base such as triethylamine, DIEA at 0° C. to room temperature for 30 minutes to 12 hours.
  • the compound (XVII) can be given by the reaction of the compound (XXII) with a corresponding alcohol, carboxylic acid, phenol, amine, thiol, thiophenol (IV) in an organic solvent such as DMF, THF, ethanol in the presence of a base such as potassium carbonate, sodium hydride at 0° C. to 100° C. for 1 hour to 48 hours.
  • the compound (XVIII) can be given by the reaction of the compound (XVII) with a corresponding diboron (XXIII) or borane (XXIV) in a solvent such as dimethylsulfoxide, DMF, 1,4-dioxane in the presence of a base such as potassium acetate, triethylamine and a catalyst such as [1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloride, bis(triphenylphosphine)palladium (II) dichloride at 50° C. to 120° C. for 10 minutes to 48 hours.
  • a solvent such as dimethylsulfoxide, DMF, 1,4-dioxane
  • a base such as potassium acetate
  • triethylamine triethylamine
  • a catalyst such as [1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloride,
  • the present compound (I)-(d) (the compound that A is methylene group, X is O, one of R 1 is OR 10 , R 10 is a lower alkyl group which may have at least a substituent, a lower alkylcarbonyl group which may have at least a substituent, an arylcarbonyl group which may have at least a substituent, a heterocyclic carbonyl group which may have at least a substituent, a lower alkoxycarbonyl group which may have at least a substituent or an aryloxycarbonyl group which may have at least a substituent, and the like in the general formula (1)) can be synthesized according to the synthetic route 9.
  • the compound (I)-(d) can be given by the reaction of the present compound (I)-(e) (the compound that A is methylene group, X is O, one of R 1 is OH in the general formula (1)) with a corresponding halide (XXV) in an organic solvent such as THF, methylene dichloride, DMF in the presence of a base such as triethylamine, DIEA, potassium carbonate at 0° C. to 100° C. for 1 hour to 24 hours.
  • a base such as triethylamine, DIEA
  • the present compound (I)-(f) (the compound that A is methylene group, X is O, one of the R 1 is OCOR 11 , R 11 is a lower alkyl group which may have at least a substituent, an aryl group which may have at least a substituent or a heterocyclic group which may have at least a substituent, and the like in the general formula (1)) can be synthesized according to the synthetic route 10.
  • the compound (I)-(f) can be given by the reaction of the present compound (I)-(e) (the compound that A is methylene group, X is O, one of R 1 is OH in the general formula (1)) with a corresponding carboxylic acid (XXVI) in an organic solvent such as DMF, methylene dichloride in the presence of a condensation agent such as N,N′-dicyclohexylcarbodiimide (hereinafter referred to as DCC), O-(7-azabenzotriazol-1-yl)-N,N,N,N-tetramethyl uroniumhexafluorophosphate (hereinafter referred to as HATU) and a base such as DIEA at room temperature to 50° C. for 1 hour to 3 days.
  • a condensation agent such as N,N′-dicyclohexylcarbodiimide (hereinafter referred to as DCC)
  • HATU O-(7-azabenzotriazol-1-y
  • the present compound (I)-(g) (the compound that A is methylene group, X is O, one of the R 1 is OCONR 12 R 13 , R 12 and R 13 may be the same or different and are a lower alkyl group which may have at least a substituent, an aryl group which may have at least a substituent, and the like in the general formula (1)) can be synthesized according to the synthetic route 11.
  • the compound (I)-(g) can be given by the reaction of the present compound (I)-(e) (the compound that A is methylene group, X is O, one of the R 1 is OH in the general formula (1)) with 1,1′-carbonyldiimidazole (hereinafter referred to as CDI) in an organic solvent such as methylene dichloride, THF at room temperature to 50° C. for 30 minutes to 12 hours followed by the reaction with a corresponding amine (XXVII).
  • CDI 1,1′-carbonyldiimidazole
  • the present compound (I)-(e) (the compound that A is methylene group, X is O, one of the R 1 is OH in the general formula (1)) can be synthesized according to the synthetic route 12. Namely, the present compound (I)-(h) can be given by the reaction of the compound (XVII) with a corresponding boronic acid or its ester (XXVIII) in a solvent such as DMF, 1,4-dioxane, ethanol, toluene, water in the presence of a base such as cesium carbonate, sodium carbonate, sodium hydrogen carbonate, tripotassium phosphate and a catalyst such as bis(triphenylphosphine)palladium (II) dichloride, tetrakis(triphenylphosphine)palladium (0) at 50° C.
  • a solvent such as DMF, 1,4-dioxane, ethanol, toluene
  • a base such as cesium carbonate, sodium carbonate
  • the compound (I)-(e) can be given by the treatment of the compound (I)-(h) in an organic solvent such as 1,4-dioxane, methylene dichloride in the presence of an acid such as hydrogen chloride, trifluoroacetic acid at 0° C. to 50° C. for 1 hour to 24 hours.
  • an organic solvent such as 1,4-dioxane, methylene dichloride
  • an acid such as hydrogen chloride, trifluoroacetic acid at 0° C. to 50° C. for 1 hour to 24 hours.
  • the present compound (I)-(e) (the compound that A is methylene group, X is O, one of the R 1 is OH in the general formula (1)) can be also synthesized according to the synthetic route 13.
  • the compound (XXIX) can be given by the reaction of the compound (VII) with a corresponding boronic acid or its ester (XXVIII) in a solvent such as DMF, 1,4-dioxane, ethanol, toluene, water in the presence of a base such as cesium carbonate, sodium carbonate, sodium hydrogen carbonate, tripotassium phosphate and a catalyst such as bis(triphenylphosphine)palladium (II) dichloride, tetrakis(triphenylphosphine)palladium (0) at 50° C.
  • the compound (XXX) can be given by the treatment of the compound (XXIX) in an organic solvent such as diethylether, THF in the presence of a reductive agent such as lithium aluminium hydride at ⁇ 30° C. to room temperature for 1 hour to 24 hours.
  • the compound (XXXI) can be given by the treatment of the compound (XXX) with methanesulfonyl chloride in an organic solvent such as methylene dichloride, THF in the presence of a base such as triethylamine, DIEA at 0° C. to room temperature for 30 minutes to 12 hours.
  • the present compound (I)-(i) can be given by the reaction of the compound (XXXI) with a corresponding alcohol, carboxylic acid, phenol, amine, thiol, thiophenol and the like (IV) in an organic solvent such as DMF, THF, ethanol in the presence of a base such as potassium carbonate, sodium hydride at 0° C. to 100° C. for 1 hour to 48 hours.
  • a base such as potassium carbonate, sodium hydride at 0° C. to 100° C. for 1 hour to 48 hours.
  • the present compound (I)-(h) can be given by the reaction of the compound (I)-(i) with a corresponding halide (II) in an organic solvent such as DMF, THF, 1,4-dioxane, methylene dichloride in the presence of a base such as cesium carbonate, potassium carbonate at 0° C. to 50° C. for 1 hour to 24 hours.
  • the compound (I)-(e) can be given by the treatment of the compound (I)-(h) in an organic solvent such as 1,4-dioxane, methylene dichloride in the presence of an acid such as hydrogen chloride, trifluoroacetic acid at 0° C. to 50° C. for 1 hour to 24 hours.
  • the present compound (I)-(j) (the compound that A is methylene group, X is O, one of the R 1 is OR 10 , R 7 is NHR 8 , R 10 is a lower alkyl group which may have at least a substituent, a lower alkylcarbonyl group which may have at least a substituent, an arylcarbonyl group which may have at least a substituent, a heterocyclic carbonyl group which may have at least a substituent, a lower alkoxycarbonyl group which may have at least a substituent, an aryloxycarbonyl group which may have at least a substituent, and the like in the general formula (1)), the present compound (I)-(k) (the compound that A is methylene group, X is O, one of the R 1 is OCOR 11 , R 7 is NHR 8 , R 1 ′′ is a lower alkyl group which may have at least a substituent, an aryl group which may have at least a substituent, a
  • the compound (I)-(j), (I)-(k) and (I)-(l) can be given by the reaction of the present compound (I)-(m) (the compound that A is methylene group, X is O, one of the R 1 is OH, R 7 is NR 8 (Fmoc) in the general formula (1)) with a corresponding halide (XXV), a carboxylic acid (XXVI) or an amine (XXVII) according to the method of synthetic route 9, 10 or 11 respectively, followed by the treatment in an organic solvent such as DMF, methylene dichloride in the presence of a base such as piperidine at 0° C. to 50° C. for 5 minutes to 24 hours.
  • an organic solvent such as DMF
  • methylene dichloride in the presence of a base such as piperidine at 0° C. to 50° C. for 5 minutes to 24 hours.
  • the present compound (I)-(m) (the compound that A is methylene group, X is O, one of the R 1 is OH, R 7 is NR 8 (Fmoc) in the general formula (1)) can be synthesized according to the synthetic route 15.
  • the compound (XXXIII) can be given by the reaction of the compound (XXII) with a corresponding amine (XXXII) in an organic solvent such as DMF, THF, ethanol in the presence of a base such as potassium carbonate, sodium hydride at 0° C. to 100° C. for 1 hour to 48 hours.
  • the present compound (I)-(o) can be given by the reaction of the compound (XXXIII) with a corresponding boronic acid or its ester (XXVIII) in a solvent such as DMF, 1,4-dioxane, ethanol, toluene, water in the presence of a base such as cesium carbonate, sodium carbonate, sodium hydrogen carbonate, tripotassium phosphate and a catalyst such as bis(triphenylphosphine)palladium (II) dichloride, tetrakis(triphenylphosphine)palladium (0) at 50° C. to 120° C. for 1 hour to 48 hours.
  • a solvent such as DMF, 1,4-dioxane, ethanol, toluene
  • a base such as cesium carbonate, sodium carbonate, sodium hydrogen carbonate, tripotassium phosphate
  • a catalyst such as bis(triphenylphosphine)palladium (II) dichlor
  • the present compound (I)-(n) can be given by the reaction of the compound (I)-(o) with 9-fluorenylmethoxycarbonyl chloride in a solvent such as 1,4-dioxane, water in the presence of a base such as sodium hydrogen carbonate at 0° C. to 50° C. for 1 hour to 24 hours.
  • the compound (I)-(m) can be given by the treatment of the compound (I)-(n) in an organic solvent such as 1,4-dioxane, methylene dichloride in the presence of an acid such as hydrogen chloride, trifluoroacetic acid at 0° C. to 50° C. for 1 hour to 24 hours.
  • the present compound (I)-(p) (the compound that A is methylene group, X is O, one of the R 1 is OR 10 , R 7 is OR 8 , R 10 is a lower alkyl group which may have at least a substituent, a lower alkylcarbonyl group which may have at least a substituent, an arylcarbonyl group which may have at least a substituent, a heterocyclic carbonyl group which may have at least a substituent, a lower alkoxycarbonyl group which may have at least a substituent, an aryloxycarbonyl group which may have at least a substituent, and the like in the general formula (1)) can be synthesized according to the synthetic route 16.
  • the compound (XXXIV) can be given by the treatment of the compound (XXX) in an organic solvent such as 1,4-dioxane, methylene dichloride in the presence of an acid such as hydrogen chloride, trifluoroacetic acid at 0° C. to 50° C. for 1 hour to 24 hours.
  • the compound (XXXV) can be given by the reaction of the compound (XXXIV) with a corresponding halide (XXV) in an organic solvent such as THF, methylene dichloride, DMF in the presence of a base such as triethylamine, DIEA, potassium carbonate at 0° C. to 100° C. for 1 hour to 24 hours.
  • the compound (I)-(q) can be given by the reaction of the compound (XXXV) with a corresponding halide (VI) in an organic solvent such as DMF, THF, methylene dichloride in the presence of a base such as triethylamine, potassium carbonate at 0° C. to 50° C. for 1 hour to 48 hours.
  • the compound (I)-(p) can be given by the reaction of the compound (I)-(q) with a corresponding halide (II) in an organic solvent such as DMF, THF, 1,4-dioxane, methylene dichloride in the presence of a base such as cesium carbonate, potassium carbonate at 0° C. to 50° C. for 1 hour to 24 hours.
  • the present invention also relates to a method of preventing or treating a glucocorticoid receptor-related disease, for example, metabolic disorders such as diabetes and obesity, inflammatory diseases such as arthritis, enteritis and chronic obstructive pulmonary diseases, autoimmune diseases such as connective tissue diseases, allergic diseases such as asthma, atopic dermatitis, allergic rhinitis and conjunctivitis, central nervous system diseases such as psychiatric disorders, Alzheimer's disease and drug use disorders, cardiovascular diseases such as hypertension, hypercalcemia, hyperinsulinemia and hyperlipidemia, homeostasis-related diseases causing an abnormality of neuro-immune-endocrine balance, glaucoma, comprising administering to a patient a therapeutically effective amount of the present compound or a salt thereof.
  • a glucocorticoid receptor-related disease for example, metabolic disorders such as diabetes and obesity, inflammatory diseases such as arthritis, enteritis and chronic obstructive pulmonary diseases, autoimmune diseases such as connective tissue diseases
  • glucocorticoid receptor competitor assay kit In order to find the usefulness of the present compound as a pharmaceutical, by using a glucocorticoid receptor competitor assay kit, a glucocorticoid receptor competitor assay was carried out by a fluorescence polarization method. As a result, the present compound showed an excellent glucocorticoid receptor binding activity.
  • the glucocorticoid receptor is associated with the occurrence of various diseases as described above, therefore, the present compound having an excellent binding activity to the glucocorticoid receptor is useful as a glucocorticoid receptor modulator.
  • the present compound can be administered either orally or parenterally.
  • the dosage form include a tablet, a capsule, a granule, a powder, an injection, an eye drop and the like.
  • Such a preparation can be prepared using a commonly used technique.
  • an oral preparation such as a tablet, a capsule, a granule or a powder can be prepared by optionally adding a necessary amount of an excipient such as lactose, mannitol, starch, crystalline cellulose, light silicic anhydride, calcium carbonate or calcium hydrogen phosphate; a lubricant such as stearic acid, magnesium stearate or talc; a binder such as starch, hydroxypropyl cellulose, hydroxypropylmethyl cellulose or polyvinylpyrrolidone; a disintegrant such as carboxymethyl cellulose, low-substituted hydroxypropylmethyl cellulose or calcium citrate; a coating agent such as hydroxypropylmethyl cellulose, macrogol or a silicone resin; a stabilizer such as ethyl p-hydroxybenzoate or benzyl alcohol; a corrigent such as a sweetener, a sour agent or a flavor, or the like.
  • an excipient such
  • a parenteral preparation such as an injection or an eye drop can be prepared by optionally adding a necessary amount of a tonicity agent such as sodium chloride, concentrated glycerin, propylene glycol, polyethylene glycol, potassium chloride, sorbitol or mannitol; a buffer such as sodium phosphate, sodium hydrogen phosphate, sodium acetate, citric acid, glacial acetic acid or trometamol; a surfactant such as polyoxyethylene sorbitan monoolate, polyoxy 40 stearate or polyoxyethylene hydrogenated castor oil 60; a stabilizer such as sodium citrate or sodium edetate; a preservative such as benzalkonium chloride, paraben, benzothonium chloride, p-hydroxybenzoate ester, sodium benzoate or chlorobutanol; a pH adjusting agent such as hydrochloric acid, citric acid, phosphoric acid, glacial acetic acid, sodium hydroxide, sodium carbonate or sodium hydrogen carbonate;
  • the dose of the present compound can be appropriately selected depending on the symptoms, age, dosage form or the like.
  • an oral preparation it can be administered in an amount of generally 0.01 to 1000 mg, preferably 1 to 100 mg per day in a single dose or several divided doses.
  • a preparation containing the present compound at a concentration of generally 0.0001% to 10% (w/v), preferably 0.01% to 5% (w/v) can be administered in a single dose or several divided doses.
  • Fmoc in the chemical structure in Production Examples represents 9-fluorenylmethoxycarbonyl group.
  • Methyl 5-amino-2-bromobenzoate (Reference Compound No. 1-(1), 21.0 g, 91.2 mmol) was dissolved in anhydrous dichloromethane (450 mL), triethylamine (19.0 mL, 137 mmol) and acethyl chloride (13.0 mL, 182 mmol) were added dropwise over 30 minutes successively, and then the mixture was stirred at 0° C. for 2 hours.
  • Lithium aluminium hydride (26.0 mg, 0.64 mmol) was suspended in anhydrous tetrahydrofuran (0.5 mL) under nitrogen atmosphere.
  • An anhydrous tetrahydrofuran solution (1.5 mL) of 8-methoxycarbonyl-7-(2-methoxyphenyl)-3,3-dimethyl-3,4-dihydro-1H-quinoxalin-2-one (Reference Compound No. 2-1, 108 mg, 0.32 mmol) was added thereto at 0° C., and stirred for 3 hours at the same temperature.
  • Litium aluminium hydride (38.5 mg, 1.01 mmol) was suspended in anhydrous tetrahydrofuran (0.5 mL) under nitrogen atmosphere.
  • An anhydrous tetrahydrofuran solution (1.5 mL) of 7-bromo-8-methoxycarbonyl-3,3-dimethyl-3,4-dihydro-1H-quinoxalin-2-one (Reference Compound No. 1, 101 mg, 0.323 mmol) was added dropwise thereto at 0° C., and stirred for 1 hour at the same temperature.
  • Ethyl acetate (10 mL), water (10 mL), and 1N aqueous hydrochloride solution (2 mL) were added thereto successively and the mixture was partitioned.
  • Lithium aluminium hydride (442 mg, 11.7 mmol) was suspended in anhydrous tetrahydrofuran (10 mL) under nitrogen atmosphere.
  • An anhydrous tetrahydrofuran solution (40 mL) of 9-chloro-2,2,4-trimethyl-1,4-dihydro-2H-6-oxa-1,4-diazachrysen-3,5-dione (Reference Compound No. 11-1, 1.99 g, 5.81 mmol) was added dropwise thereto at ⁇ 10° C. and stirred for 10 minutes at the same temperature.
  • a tablet of the above-mentioned formulation is coated with 3 mg of a coating agent (for example, a conventional coating agent such as hydroxypropylmethyl cellulose, macrogol or a silicone resin), whereby an objective tablet can be obtained.
  • a coating agent for example, a conventional coating agent such as hydroxypropylmethyl cellulose, macrogol or a silicone resin
  • a desired tablet can be obtained by appropriately changing the kind and/or amount of the present compound and additives.
  • a desired capsule can be obtained by appropriately changing the kind and/or amount of the present compound and additives.
  • a desired eye drop can be obtained by appropriately changing the kind and/or amount of the present compound and additives.
  • a receptor competitor assay was carried out by a fluorescence polarization method.
  • a GR competitor assay kit manufactured by Invitrogen, cat No. P2816 was used, and a procedure was carried out according to the protocol attached to the kit.
  • the specific method will be described.
  • GR screening buffer A buffer containing 10 mM potassium phosphate (pH 7.4), 20 mM sodium molybdate (Na 2 MoO 4 ), 0.1 mM ethylene diamine tetraacetic acid (EDTA), 5 mM dithiothreitol (DTT), 0.1 mM stabilizing peptide and 2% dimethylsulfoxide was prepared.
  • FluormoneTM GS1 which is a fluorescent glucocorticoid ligand, was diluted with GR screening buffer, whereby a 4 nM solution was prepared.
  • Recombinant human GR was diluted with GR screening buffer, whereby a 16 nM solution was prepared.
  • test compound solution was prepared.
  • test compound solution was added in an amount of 25 ⁇ L into each well of a 96-well plate, and then, 4 ⁇ GS1 solution and 4 ⁇ GR solution were added in an amount of 12.5 ⁇ L into each well, respectively.
  • a GR binding ratio (%) was calculated from the following equation.
  • GR binding ratio (%) 100 ⁇ [1-(fluorescence polarization of test compound solution-fluorescence polarization of positive control solution)/(fluorescence polarization of negative control solution—fluorescence polarization of positive control solution)]
  • the GR binding ratios (%) of the test compounds (Compound 1-4, Compound 2-2, Compound 2-9, Compound 2-16, Compound 3-7, Compound 3-10, Compound 3-15, Compound 3-16, Compound 3-17, Compound 4-5, Compound 4-7, Compound 4-10, Compound 4-11, Compound 5-1, Compound 5-9, Compound 5-14, Compound 5-18, Compound 5-19, Compound 5-21, Compound 5-22, Compound 5-24, Compound 6-4, Compound 6-8, Compound 6-10, Compound 6-12, Compound 6-15, Compound 6-19, Compound 6-23, Compound 6-27, Compound 6-32, Compound 6-38, Compound 8-2, Compound 9-1, Compound 11, Compound 13-2, Compound 14-2, Compound 14-4, Compound 14-11, Compound 14-21, Compound 14-22, Compound 14-30, Compound 14-33, Compound 14-35, Compound 14-36, Compound 14-37, Compound 14-44, Com
  • the present compound showed an excellent GR binding activity. Accordingly, the present compound can be used as a GR modulator, and is useful for a preventive or therapeutic agent particularly for GR-related diseases, that is, metabolic disorders, inflammatory diseases, autoimmune diseases, allergic diseases, central nervous system diseases, cardiovascular diseases, homeostasis-related diseases, glaucoma and the like.
  • GR-related diseases that is, metabolic disorders, inflammatory diseases, autoimmune diseases, allergic diseases, central nervous system diseases, cardiovascular diseases, homeostasis-related diseases, glaucoma and the like.
  • 1,2,3,4-tetrahydroquinoxaline derivative or the salt according to the present invention has a binding activity to GR and is useful for GR modulator of nonsteroidal compound.

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